The aim of the this study was to compare the in vitro developmental competence of parthenogenetically activated oocytes cryopreserved with slow-freezing or vitrification. Supernumerary metaphase II oocytes obtained during in vitro fertilization procedures were randomized to slow freezing or vitrification procedure. After thawing or devitrification, oocytes were parthenogenetically activated and cultured. Survival, activation, development rate, and cell number during culture were compared. The 2 groups showed no significant differences between the rates of parthenogenetic activation, development, good quality parthenotes and blastomere number on day 2 of culture. However, parthenotes from the devitrified oocytes continued cleaving till day 3...
PURPOSE: This study aims to determine if in-vitro maturation (IVM) of human immature oocytes should ...
INTRODUCTION: Oocyte cryopreservation protocols have not been fully optimized yet and overall clinic...
OBJECTIVE: To compare directly in vitro developmental competence between parthenogenetically activat...
Objective: This study compared spindles, cytoskeleton, and developmental potential between vitrified...
Preservation of female genetics is currently done primarily by means of oocyte and embryo cryopreser...
SummaryBoth the slow-freezing method with increased sucrose concentration and new vitrification tech...
AbstractNowadays, human oocytes/embryos are cryopreserved via slow freezing or vitrification. The ai...
Both the slow-freezing method with increased sucrose concentration and new vitrification techniques ...
Background/Aims: To observe the effects of vitrification on spindle, zona pellucida, embryonic aneup...
How does the in vitro maturation (IVM) medium and the vitrification procedure affect the survival of...
This study investigated whether failed maturation oocytes could be used to evaluate different cryopr...
Abstract: Heat transfer during cooling and warming is difficult to measure in cryo-devices; mathemat...
The oocyte cryopreservation is more promising than embryo freezing in clinical applications, preserv...
The aim of this work is the comparison of cryoprotection methods for human oocytes regarding their s...
Abstract Background Oocyte cryopreservation is an important method used in a number of human fertili...
PURPOSE: This study aims to determine if in-vitro maturation (IVM) of human immature oocytes should ...
INTRODUCTION: Oocyte cryopreservation protocols have not been fully optimized yet and overall clinic...
OBJECTIVE: To compare directly in vitro developmental competence between parthenogenetically activat...
Objective: This study compared spindles, cytoskeleton, and developmental potential between vitrified...
Preservation of female genetics is currently done primarily by means of oocyte and embryo cryopreser...
SummaryBoth the slow-freezing method with increased sucrose concentration and new vitrification tech...
AbstractNowadays, human oocytes/embryos are cryopreserved via slow freezing or vitrification. The ai...
Both the slow-freezing method with increased sucrose concentration and new vitrification techniques ...
Background/Aims: To observe the effects of vitrification on spindle, zona pellucida, embryonic aneup...
How does the in vitro maturation (IVM) medium and the vitrification procedure affect the survival of...
This study investigated whether failed maturation oocytes could be used to evaluate different cryopr...
Abstract: Heat transfer during cooling and warming is difficult to measure in cryo-devices; mathemat...
The oocyte cryopreservation is more promising than embryo freezing in clinical applications, preserv...
The aim of this work is the comparison of cryoprotection methods for human oocytes regarding their s...
Abstract Background Oocyte cryopreservation is an important method used in a number of human fertili...
PURPOSE: This study aims to determine if in-vitro maturation (IVM) of human immature oocytes should ...
INTRODUCTION: Oocyte cryopreservation protocols have not been fully optimized yet and overall clinic...
OBJECTIVE: To compare directly in vitro developmental competence between parthenogenetically activat...